Evidence map›Paper›PMID 19175750›Full record

ArticleNeurogastroenterology and motility2009

Interstitial cells of Cajal contain signalling molecules for transduction of nitrergic stimulation in guinea pig caecum.

S Iino, K Horiguchi, Y Nojyo, S M Ward, K M Sanders

Abstract read
In one paragraph

Article in Neurogastroenterology and motility, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.0field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. CaAdvances in experimental medicine and biology · 2022
    Article
  7. Review
  8. Article
  9. Review
  10. Inhibitory Neural Regulation of the CaFrontiers in physiology · 2018
    Article
  11. R-Type CaExperimental physiology · 2017
    Article
  12. Article
  13. Convergence of inhibitory neural inputs regulate motor activity in the murine and monkey stomach.American journal of physiology. Gastrointestinal and liver physiology · 2016
    Article
  14. Article
  15. Enteric Inhibitory Neurotransmission, Starting Down Under.Advances in experimental medicine and biology · 2016
    Review
  16. Article
  17. Article
  18. The significance of interstitial cells in neurogastroenterology.Journal of neurogastroenterology and motility · 2014
    Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

S IinoDepartment of Morphological and Physiological Sciences, University of Fukui Faculty of Medical Sciences, Eiheiji, Fukui, Japan. iinosa@u-fukui.ac.jp
K Horiguchi
Y Nojyo
S M Ward
K M Sanders
University of Fukui · JPUniversity of Nevada, Reno · US

Funding

Tissue, Cell and Tissue Culture CoreP01DK041315 · NIDDK · UNIVERSITY OF NEVADA RENO · PI WARD, SEAN M · 1989 to 2018
$26.3M
NIDDK NIH HHS P01 DK041315NIDDK NIH HHS P01 DK41315
6 · The paper itself

Abstract

Nitric oxide (NO) is an inhibitory signalling molecule in the gastrointestinal (GI) tract that is released from neurons and from leucocytes during inflammation. NO stimulates soluble guanylate cyclase (sGC), elevates cyclic guanosine 3',5'-monophospate (cGMP), and subsequently activates cGMP-dependent protein kinase (PKG). Targets for NO in the guinea pig caecum were investigated by characterizing the cellular distribution of sGC, cGMP and PKG. Immunoreactivity for both isoforms of sGC, sGCalpha1 and sGCbeta1, was observed in the interstitial cells of Cajal (ICC) and enteric neurons in the tunica muscularis. Double labelling with anti-Kit and anti-sGC antibodies showed sGCalpha1 and sGCbeta1-like immunoreactivity (LI) in almost all intramuscular (IM) and myenteric ICC. Neuronal processes with neuronal NO synthase were closely apposed to ICC expressing sGC-LI. Cells with sGC-LI possessed ultrastructural features of ICC-IM: caveolae, close association with nerve bundles and contacts with smooth muscle cells (SMC). Sodium nitroprusside, added with the phosphodiesterase inhibitors (3-isobutyl-1-methylxanthine and zaprinast), enhanced cGMP-LI in almost all ICC and in some enteric neurons. Nerve stimulation also increased cGMP-LI in ICC and enteric neurons. In contrast, no resolvable increase in cGMP-LI was observed in any cells when the sGC inhibitor 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one was present. ICC and SMC also expressed PKG type I-LI. These data show that ICC express the downstream signalling molecules necessary to transduce nitrergic signals and activate inhibitory pathways and thus are primary targets for NO released from neurons and other cells in the GI tract.

Indexed as

CecumAnimalsCyclic GMPCyclic GMP-Dependent Protein KinasesEnzyme ActivationFemaleGuanylate CyclaseGuinea PigsHumansIsoenzymesMiceMice, Inbred BALB CNitric OxideNitric Oxide Synthase Type INitroprussidePhosphodiesterase InhibitorsCyclic GMPCyclic GMP-Dependent Protein KinasesGuanylate CyclaseIsoenzymesNitric OxideNitric Oxide Synthase Type INitroprussidePhosphodiesterase InhibitorsPurinonesReceptors, Cytoplasmic and NuclearSoluble Guanylyl CyclaseStem Cell Factorzaprinast

Identifiers

PMID19175750
PMCPMC4793909
OpenAlexW1986625535

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.